RESUMO Objetivo: Fenótipos Stargardt-like já foram asso-ciados a variantes patogênicas no gene ABCA4. O propósito desse estudo é descrever quatro pacientes com achados retinianos semelhantes a doença de Stargardt com resultados moleculares diferentes do esperado. Métodos: Esse relato fez a revisão de prontuários médicos de quatro pacientes com distrofia macular e achados clínicos sugestivos de doença de Stargardt. Foram realizados avaliação oftalmológica, exames de imagens e testes usando next generation sequencing para avaliar variantes patogênicas associadas aos fenótipos dos pacientes. Resultados: Os pacientes apresentavam atrofia macular e alterações pigmentares sugerindo achados clínicos de doença de Stargardt. Dois pacientes foram associados a genes com herança autossômica dominante (RIMS1 e CRX) e dois pacientes foram associados a genes com herança autossômica recessiva (CRB1 e RDH12) com variantes preditoras de serem patogênicas. Conclusão: Distrofias maculares podem ter similaridades fenotípicas com fenótipo de Stargardt-like associados a outros genes além dos classicamente já descritos. Objetivo Stargardtlike like asso ciados ABCA4 ABCA esperado Métodos oftalmológica Resultados RIMS1 RIMS (RIMS CRX CRB1 CRB (CRB RDH12 RDH Conclusão descritos RDH1

ABSTRACT Purpose: Stargardt-like phenotype has been described as associated with pathogenic variants besides the ABCA4 gene. This study aimed to describe four cases with retinal appearance of Stargardt disease phenotypes and unexpected molecular findings. Methods: This report reviewed medical records of four patients with macular dystrophy and clinical features of Stargardt disease. Ophthalmic examination, fundus imaging, and next-generation sequencing were performed to evaluate pathogenic variants related to the phenotypes. Results: Patients presented macular atrophy and pigmentary changes suggesting Stargardt disease. The phenotypes of the two patients were associated with autosomal dominant inheritance pattern genes (RIMS1 and CRX) and in the other two patients were associated with recessive dominant inheritance pattern genes (CRB1 and RDH12) with variants predicted to be pathogenic. Conclusion: Macular dystrophies may have phenotypic similarities to Stargardt-like phenotype associated with other genes besides the classic ones. Purpose Stargardtlike like ABCA gene findings Methods examination imaging nextgeneration next generation Results RIMS1 RIMS (RIMS CRX CRB1 CRB (CRB RDH12 RDH Conclusion ones RDH1

RESUMO Objetivo: Fenótipos Stargardt-like já foram asso-ciados a variantes patogênicas no gene ABCA4. O propósito desse estudo é descrever quatro pacientes com achados retinianos semelhantes a doença de Stargardt com resultados moleculares diferentes do esperado. Métodos: Esse relato fez a revisão de prontuários médicos de quatro pacientes com distrofia macular e achados clínicos sugestivos de doença de Stargardt. Foram realizados avaliação oftalmológica, exames de imagens e testes usando next generation sequencing para avaliar variantes patogênicas associadas aos fenótipos dos pacientes. Resultados: Os pacientes apresentavam atrofia macular e alterações pigmentares sugerindo achados clínicos de doença de Stargardt. Dois pacientes foram associados a genes com herança autossômica dominante (RIMS1 e CRX) e dois pacientes foram associados a genes com herança autossômica recessiva (CRB1 e RDH12) com variantes preditoras de serem patogênicas. Conclusão: Distrofias maculares podem ter similaridades fenotípicas com fenótipo de Stargardt-like associados a outros genes além dos classicamente já descritos.

ABSTRACT Purpose: Stargardt-like phenotype has been described as associated with pathogenic variants besides the ABCA4 gene. This study aimed to describe four cases with retinal appearance of Stargardt disease phenotypes and unexpected molecular findings. Methods: This report reviewed medical records of four patients with macular dystrophy and clinical features of Stargardt disease. Ophthalmic examination, fundus imaging, and next-generation sequencing were performed to evaluate pathogenic variants related to the phenotypes. Results: Patients presented macular atrophy and pigmentary changes suggesting Stargardt disease. The phenotypes of the two patients were associated with autosomal dominant inheritance pattern genes (RIMS1 and CRX) and in the other two patients were associated with recessive dominant inheritance pattern genes (CRB1 and RDH12) with variants predicted to be pathogenic. Conclusion: Macular dystrophies may have phenotypic similarities to Stargardt-like phenotype associated with other genes besides the classic ones.

Abstract Pseudomonas fluorescens is known to have the ability to adhere and produce biofilm. The formation of biofilms is enhanced by cellular motility, particularly when mediated by flagella. Biofilm formed on surfaces such as those used for food production act as points of contamination, releasing pathogenic or deteriorating microorganisms and compromising the quality of products. We assessed two strains of Pseudomonas fluorescens PL5.4 and PL7.1, sampled from raw, chilled, buffalo milk, which was obtained from a dairy farm. Twitching and swarming motility assays were performed, in addition to the biofilm production evaluations at a temperature of 7 °C. Regarding the motility assays, only the PL5.4 strain scored positive for the swarming assay. On microplates, both strains presented themselves as strong biofilm producers at 7 °C. The PL5.4 strain was also able to form biofilm on a stainless steel structure and maintain this structure for up to 72 hours at refrigeration. The Pseudomonas fluorescens PL5.4 isolate was identified on the basis of a 99% sequence identity with Pseudomonas fluorescens A506, a strain used as a biocontrol in agriculture. Biofilm-forming bacteria, when adapted to low temperatures, become a constant source of contamination, damaging the production, quality, safety and shelf-life of products.

RESUMO A retomada às atividades odontológicas em tempos de pandemia tem sido um desafio devido à geração e dispersão de gotículas e aerossóis que podem conter o vírus SARS-CoV-2, agente etiológico da covid-19. Nos últimos meses algumas estratégias de contenção de gotículas e aerossóis tem circulado pela internet, mas a eficácia destas barreiras ainda não apresenta um bom nível de evidência na Literatura. Desta forma, e utilizando um modelo de dispersão microbiana, o objetivo deste estudo preliminar foi comparar a dispersão da alta rotação (AR) sem ou associada a uma barreira individual de biossegurança odontológica (AR / BIBO) que consiste em um bastidor acoplado ao filme de PVC e TNT. A turbina da alta rotação foi ativada durante um minuto em uma solução de Lactobacillus casei Shirota, a qual havia sido previamente acrescentada no reservatório de refrigeração de um equipamento odontológico, e placas de petri contendo ágar MRS foram posicionadas a partir do apoio de cabeça de uma cadeira odontológica nas distâncias de 50, 100 e 150 cm em diferentes ângulos (90 e 0 graus). Na distância de 50 cm, a média (desvio padrão) de L. casei Shirota para AR foi de 13.554,59 (493,48) UFC, enquanto a associação AR/BIBO foi de 570,67 (60,54) UFC, estabelecendo uma redução de 96% (p<0,0001). Considerando estes resultados preliminares e o modelo de estudo utilizado, a barreira individual de biossegurança odontológica se mostrou eficiente em reduzir a dispersão da turbina de alta rotação, o que sugere que o seu uso pode ser uma alternativa para a melhoria da biossegurança em ambiente odontológico.

ABSTRACT The return to dental practice in pandemic times is a new challenge due to the generation and dispersion of droplets and aerosols that may contain the SARS-CoV-2 virus, the etiological agent of covid-19. In the last months some droplet and aerosol containment strategies have been circulating on the internet, however, until now there is no evidence in the literature to prove the effectiveness of such barriers. Thus, using a microbial dispersion model with the fast handpiece, the aim of this preliminary study was to compare the dispersion caused by the the dental drill (DD) alone or in association with an individual biosafety barrier (IDBD / DD), which consisted of a layer of PVC film combined to a layer of polypropylene mounted on a frame. The dental drill was activated for one minute having had the water from the reservoir been replaced with a suspension of Lactobacillus casei Shirota. Petri dishes containing MRS agar were positioned at 50, 100 and 150 cm from the headboard of the dental chair at different angles (90 and 0 degrees). At 50 cm, the mean (standard deviation) of L. casei Shirota for DD was 13,554.59 (493.48) CFU, while for IDBD / DD was 570.67 (60.54) CFU (p <0.0001), establishing a 96% reduction. Considering these preliminary results, the individual biosafety barrier proved effective in reducing dispersion from the dental drill in this study model, which suggests that this barrier may be a viable option to optimize biosafety in the dental environment.

As terapias celulares para doenças neurológicas têm avançado e células precursoras neurais (NPC) surgem como candidatas ideais para o transplante de células neurais em muitas doenças. No entanto, trabalhos adicionais devem ser feitos para determinar o ambiente de cultivo ideal para a expansão in vitro das NPC, sem alterar sua plasticidade, e os mecanismos de sinalização celular do fator de crescimento epidérmico (EGF) e fator de crescimento de fibroblasto 2 (FGF-2) no crescimento, sobrevivência e diferenciação da neuroesfera. Nesse trabalho avaliamosNPCcultivadas na presença e na ausência de FGF-2 e EGF e mostramos que esses fatores de crescimento são responsáveis pela proliferação das NPC. Também foi demonstrado que a produção endógena de fatores de crescimento alterna de FGF-2 a fator de crescimento de insulina 1 (IGF-1) e fator de crescimento derivado de plaquetas b (PDGFb) após remoção de EGF e FGF-2. NPC de camundongo cultivadas em suspensão mostraram padrões de localização neuronal distintos (centro versus borda) tanto no grupo controle como no grupo sem EGF e FGF-2. Juntos, esses resultados mostram que a remoção de EGF e FGF-2 exerce importante ação na diferenciação de NPC e possivelmente contribui para melhor compreensão dos mecanismos envolvidos na diferenciação. Nossos achados sugerem que, privando as NPC de fatores de crescimento antes do transplante, talvez aumente as chances de que as células efetivamente se integrem ao hospedeiro.

Cell therapy for neurological disorders has advanced, and neural precursor cells (NPC) may become the ideal candidates for neural transplantation in a wide range of diseases. However, additional work has to be done to determine either the ideal culture environment for NPC expansion in vitro, without altering their plasticity, or the FGF-2 and EGF mechanisms of cell signaling in neurospheres growth, survival and differentiation. In this work we evaluated mouse neurospheres cultured with and without FGF-2 and EGF containing medium and showed that those growth factors are responsible for NPC proliferation. It is also demonstrated that endogenous production of growth factors shifts from FGF-2 to IGF-1/PDGFb upon EGF and FGF-2 withdrawal. Mouse NPC cultured in suspension showed different patterns of neuronal localization (core versus shell) for both EGF and FGF-2 withdrawal and control groups. Taken together, these results show that EGF and FGF-2 removal play an important role in NPC differentiation and may contribute to a better understanding of mechanisms of NPC differentiation. Our findings suggest that depriving NPC of growth factors prior to grafting might enhance their chance to effectively integrate into the host.